Effect of L-NAME, an inhibitor of nitric oxide synthesis, on plasma levels of IL-6, IL-8, TNFα and nitrite/nitrate in human septic shock

被引:31
作者
Avontuur, JAM [1 ]
Stam, TC
Jongen-Lavrencic, M
van Amsterdam, JGC
Eggermont, AMM
Bruining, HA
机构
[1] Univ Rotterdam Hosp, Dept Surg, Rotterdam, Netherlands
[2] Netherlands Red Cross Blood Transfus Serv, Dept Autoimmune Dis, Cent Lab, Amsterdam, Netherlands
[3] Expt & Clin Immunol Lab, Amsterdam, Netherlands
[4] Natl Inst Publ Hlth & Environm, Dept Pharmacol, Bilthoven, Netherlands
关键词
sepsis; nitric oxide; nitric oxide synthase inhibition; L-NAME; cytokines;
D O I
10.1007/s001340050643
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objectives: We tested the effects of N-G-nitro-L-arginine methyl ester (L-NAME), an inhibitor of nitric oxide (NO) synthesis, on plasma levels of interleukin (IL) IL-6, IL-8, tumor necrosis factor-alpha (TNF alpha) and nitrite/nitrate (NO2-/ NO3-) in patients with severe septic shock. Design: Prospective clinical study. Setting: Surgical intensive care unit at a university hospital. Patients: 11 consecutive patients with severe septic shock. Interventions: Standard hemodynamic measurements were made and blood samples taken at intervals before, during, and after a 12-h infusion of L-NAME 1 mg.kg(-1).h(-1) for determination of plasma IL-6, IL-8, TNF alpha and NO2-/NO3- concentration. Measurements and results: Patients with sepsis had increased plasma levels of IL-6, IL-8, TNF alpha and NO2-/NO3- (p<0.05), Plasma levels of IL-6. IL-8: and NO2-/NO3- were negatively correlated with systemic vascular resistance (r = -0.62, r = -0.65, and r = -0.78, respectively, all p < 0.05). Continuous infusion of L-NAME increased mean arterial pressure and systemic vascular resistance, with a concomitant reduction in cardiac output (all p < 0.01). No significant changes were seen in levels of plasma IL-6, IL-8, and NO2-/NO3- during the 24-h observation period. Plasma levels of TNF alpha were significantly reduced during L-NAME infusion compared to baseline (p < 0.05), Conclusions: NO plays a role in the cardiovascular derangements of human septic shock. Inhibition of NO synthesis with L-NAME does not promote excessive cytokine release in patients with severe sepsis.
引用
收藏
页码:673 / 679
页数:7
相关论文
共 36 条
  • [1] Nitric oxide causes dysfunction of coronary autoregulation in endotoxemic rats
    Avontuur, JAM
    Bruining, HA
    Ince, C
    [J]. CARDIOVASCULAR RESEARCH, 1997, 35 (02) : 368 - 376
  • [2] INTERLEUKIN-8, A CHEMOTACTIC AND INFLAMMATORY CYTOKINE
    BAGGIOLINI, M
    CLARKLEWIS, I
    [J]. FEBS LETTERS, 1992, 307 (01) : 97 - 101
  • [3] BEUTLER B, 1987, NEW ENGL J MED, V316, P379
  • [4] BOCZKOWSKI J, 1995, LIFE SCI, V57, P147
  • [5] SEPSIS SYNDROME - A VALID CLINICAL ENTITY
    BONE, RC
    FISHER, CJ
    CLEMMER, TP
    SLOTMAN, GJ
    METZ, CA
    BALK, RA
    [J]. CRITICAL CARE MEDICINE, 1989, 17 (05) : 389 - 393
  • [6] Proinflammatory cytokines, measured in a mixed population on arrival in the emergency department, are related to mortality and severity of disease
    Carlstedt, F
    Lind, L
    Lindahl, B
    [J]. JOURNAL OF INTERNAL MEDICINE, 1997, 242 (05) : 361 - 365
  • [7] Role of nitric oxide in immune-mediated diseases
    Cook, HT
    Cattell, V
    [J]. CLINICAL SCIENCE, 1996, 91 (04) : 375 - 384
  • [8] THE PROTECTIVE ROLE OF ENDOGENOUSLY SYNTHESIZED NITRIC-OXIDE IN STAPHYLOCOCCAL-ENTEROTOXIN B-INDUCED SHOCK IN MICE
    FLORQUIN, S
    AMRAOUI, Z
    DUBOIS, C
    DECUYPER, J
    GOLDMAN, M
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (03) : 1153 - 1158
  • [9] Plasma proinflammatory cytokine concentrations, acute physiology and chronic health evaluation (APACHE) III scores and survival in patients in an intensive care unit
    Friedland, JS
    Porter, JC
    Daryanani, S
    Bland, JM
    Screaton, NJ
    Vesely, MJJ
    Griffin, GE
    Bennett, ED
    Remick, DG
    [J]. CRITICAL CARE MEDICINE, 1996, 24 (11) : 1775 - 1781
  • [10] FUKATSU K, 1995, ARCH SURG-CHICAGO, V130, P410